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Mass function principle

Nowadays, the star formation history (SFH), initial mass function (IMF) and detailed chemical properties have been determined for many dwarfs, both in the Local Group and outside it (e.g. Grebel, Shetrone, Tolstoy, these proceedings). This in principle allows us to base theories of late-type galaxy formation and evolution on firmer grounds, by reducing the free parameter space. [Pg.368]

Subsequently, analytical expressions for the time dependence concentration of all components in the system were obtained based on mass balance principles and also considering the reactor type, the flow rates of the feed streams, and the concentrations of substrates. Using these models we found that the basic system considered is able to perform several informationprocessing functions, such as division, rectification, and switching. [Pg.29]

At last, the double focusing sector field mass spectrometer (EBQjQ2) should briefly be addressed. This mass analyser represents a highly sophisticated early design that has rarely been used for routine analysis especially for quantification. For detailed information on the functional principle the reader is referred to respective textbooks on mass spectrometry. We mention this technique as Kajbaf et al. used EBQjQ2 for detection and identification of the QTA cimetropium and its biotransformation products from liver microsomal mixtures in offline analysis of HPLC fractions after FAB ionization [23, 62] (Table 7). [Pg.327]

Fig. 9 Functional Principle of the Synchronous Ion Shield Mass Analyzer... Fig. 9 Functional Principle of the Synchronous Ion Shield Mass Analyzer...
Figure 6.123 Functional principle of a Coriolis mass flowmeter. Figure 6.123 Functional principle of a Coriolis mass flowmeter.
The functional principle is again in line with Fig. 7.2.1. Oscillating masses and acceleration sensors are produced in the same plane and consist (depending on the micromachining technique) for example of 2-10 pm thick epitactical deposited polycrystalline silicon. [Pg.308]

Fig. 7.6.3 Function principle of the Bosch mass air-flow meter. Fig. 7.6.3 Function principle of the Bosch mass air-flow meter.
Hohne (145) pointed out that the function principle of DSC can give rise to calibration errors in case of phase transitions disturbing the steady-state conditions. The cause of this problem is the temperature dependence of the coefficients of heat transfer, leading to weak nonlinearity of the calorimeter. This results in a dependence of the calibration factor on parameters such as mass and thermal conductivity of the sample, heating rate, peak shape, and temperature. By theoretical considerations and calculations, the uncertainty of the calibration factor due to the variation of sample parameters can be 1-5%, depending on the temperature and the instrument involved. [Pg.274]

Despite the uncertainty regarding absolute rates of diffusion for noble gases in a water-filled medium, the relative rates remain a direct function of mass. In principle, for example, the extent of diffusive gas loss for any reservoir can be determined by the magnitude of fractionation of known noble gas elemental ratios using Equation (24) and the appropriate mass fractionation coefficient (Eqn. 27). [Pg.562]

There are several mass analyzers. In the following sections, the most common ones are being described with their functioning principles. [Pg.91]

Although the fundamental function principle of nanocalorimeters is not changed, the theory of such calorimeters and the mathematics for the deconvolution of the sample properties from the measurements are much more complicated than for common calorimeters. The pathway of the heat flow cannot be approximated by a one-dimensional model, and the heat capacity of the sample is often in the same order of magnitude as the heat capacity of the calorimeter system, which in many chips consists only of a very thin silicon membrane. In classical calorimeters, the calorimeter system is much larger in mass and heat capacity than the sample. This is desirable to avoid an influence of the sample on the sensitivity of the calorimeter and to keep the calibration factor a device property and free it from sample properties. [Pg.226]

Eq. (51) along with the % equations leads to a pore radius as given in Eq. (54). This equation is specifically dependent upon i and therefore any positive deviation from the straight projected line in the i plot can be interpreted as capillary filling. Initially, a probability normal mass function (PMF) in x is assumed. To go beyond this assumption is, in principle, not difficult but for the data presented here it does not seem justified. The PMF, P, is... [Pg.70]

The exceptionally characteristic symmetry possibilities which appear on the approach of two atoms lead to the suspicion that they are related to the possibilities of chemical binding which are determined by the valence rules. If we bring to mind that in the formation of the H2 molecule the decisive part consisted in the permission of a symmetric centre-of-mass function for the electrons of the two atoms—despite the Pauli principle—we are led to the following assumption ... [Pg.164]

A large number of electrons of an atom are necessarily pairwise symmetrically connected, because a state is doubly occupied with respect to the centre of-mass coordinates and only adapts to the Pauli principle through the electron spin. These electrons do not take part in valence forming right from the start. The atomic electrons, which do not belong to such two-shells, will lead to the state with anti-symmetric centre-of-mass function because of B, and are to be considered valence electrons. [Pg.166]

A key featui-e of MPC is that a dynamic model of the pi ocess is used to pi-edict futui e values of the contmlled outputs. Thei-e is considei--able flexibihty concei-ning the choice of the dynamic model. Fof example, a physical model based on fifst principles (e.g., mass and energy balances) or an empirical model coiild be selected. Also, the empirical model could be a linear model (e.g., transfer function, step response model, or state space model) or a nonhnear model (e.g., neural net model). However, most industrial applications of MPC have relied on linear empirical models, which may include simple nonlinear transformations of process variables. [Pg.740]

The mass-transfer coefficients depend on complex functions of diffii-sivity, viscosity, density, interfacial tension, and turbulence. Similarly, the mass-transfer area of the droplets depends on complex functions of viscosity, interfacial tension, density difference, extractor geometry, agitation intensity, agitator design, flow rates, and interfacial rag deposits. Only limited success has been achieved in correlating extractor performance with these basic principles. The lumped parameter deals directly with the ultimate design criterion, which is the height of an extraction tower. [Pg.1464]

For a particular primary ion and fixed experimental conditions, the scattering cross-section is a function only of the mass and atomic number of the scattering atom, and can be calculated. Thus in principle, all the terms in Eq. (3.31) except the required Na are known. RBS is, therefore, an absolute method that does not require the use of standards. [Pg.147]

For a removal attempt a molecule is selected irrespective of its orientation. To enhance the efficiency of addition attempts in cases where the system possesses a high degree of orientational order, the orientation of the molecule to be added is selected in a biased way from a distribution function. For a system of linear molecules this distribution, say, g u n ), depends on the unit vector u parallel to the molecule s symmetry axis (the so-called microscopic director [70,71]) and on the macroscopic director h which is a measure of the average orientation in the entire sample [72]. The distribution g can be chosen in various ways, depending on the physical nature of the fluid (see below). However, g u n ) must be normalized to one [73,74]. In other words, an addition is attempted with a preferred orientation of the molecule determined by the macroscopic director n of the entire simulation cell. The position of the center of mass of the molecule is again chosen randomly. According to the principle of detailed balance the probability for a realization of an addition attempt is given by [73]... [Pg.28]

An example of how information from fragmentation patterns can be used to solve structural problems is given in Worked Example 12.1. This example is a simple one, but the principles used are broadly applicable for organic structure determination by mass spectrometry. We ll see in the next section and in later chapters that specific functional groups, such as alcohols, ketones, aldehydes, and amines, show specific kinds of mass spectral fragmentations that can be interpreted to provide structural information. [Pg.413]

Given that, from the penetration theory for mass transfer across an interface, the instantaneous rale ol mass transfer is inversely proportional to the square root of the time of exposure, obtain a relationship between exposure lime in the Higbie mode and surface renewal rate in the Danckwerts model which will give the same average mass transfer rate. The age distribution function and average mass transfer rate from the Danckwerts theory must be deri ved from first principles. [Pg.857]

The concentration of gas over the active catalyst surface at location / in a pore is ai [). The pore diffusion model of Section 10.4.1 linked concentrations within the pore to the concentration at the pore mouth, a. The film resistance between the external surface of the catalyst (i.e., at the mouths of the pore) and the concentration in the bulk gas phase is frequently small. Thus, a, and the effectiveness factor depends only on diffusion within the particle. However, situations exist where the film resistance also makes a contribution to rj so that Steps 2 and 8 must be considered. This contribution can be determined using the principle of equal rates i.e., the overall reaction rate equals the rate of mass transfer across the stagnant film at the external surface of the particle. Assume A is consumed by a first-order reaction. The results of the previous section give the overall reaction rate as a function of the concentration at the external surface, a. ... [Pg.366]


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See also in sourсe #XX -- [ Pg.23 ]




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